A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018324



Internal ID19107541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:56893892..56909681hg38UCSC Ensembl
Innerchr8:57806451..57822240hg19UCSC Ensembl
Innerchr8:57969005..57984794hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3815790
hg1915790
hg1815790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7230n100
Supporting Variantsnssv3688705
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018324
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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